Canonical Allele Identifier: PA2828474081
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 589983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Asn308Ser
CA1939714
NM_001371247.1:c.923A>G